Disease #01596

Official abbreviation CMH-1
Name cardiomyopathy, hypertrophic, familial, type 1 (CMH-1)
OMIM ID 192600
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 4 genes CAV3, MYH6, MYH7, MYLK2
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 22
LOVD software ©2004-2019 Leiden University Medical Center 		There are currently no updates.